Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/A
Location

Chromosome 19: between 52691813 and 52691814 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.52691813_52691814insA

Variation displays